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Isoxsuprine Hydrochloride CAS NO 34331-89-0


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CAS No.:34331-89-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Isoxsuprine Hydrochloride CAS NO 34331-89-0 is a high-purity pharmaceutical active ingredient (API) belonging to the class of vasodilators and β-adrenergic agonists. It is critical for the formulation of medications designed to improve blood flow and treat peripheral vascular disorders. This compound is essential for pharmaceutical manufacturers and research institutions developing treatments for conditions such as Raynaud's phenomenon and cerebrovascular insufficiency.

Application

  • Pharmaceutical API: Primary active ingredient in prescription medications for vasodilation.
  • Peripheral Vascular Disease Treatment: Used in formulations to alleviate symptoms of circulatory disorders in the extremities.
  • Cerebrovascular Insufficiency Therapy: A key component in drugs aimed at improving cerebral blood flow.
  • Obstetric & Gynecological Applications: Employed in certain tocolytic agents to manage premature labor.
  • Veterinary Medicine: Used in veterinary pharmaceuticals for similar vasodilatory purposes.
  • Reference Standard: Serves as a high-purity standard for analytical testing and quality control in laboratories.
  • Research & Development: Utilized in pharmacological studies and the development of new therapeutic agents.

Basic Information

Product Name Isoxsuprine Hydrochloride
CAS No. 34331-89-0
Molecular Formula C18H23NO3·HCl
Molecular Weight 337.84 g/mol
Synonyms Isoxsuprine HCl; Vasodilan; Duvadilan; (1-(4-Hydroxyphenyl)-2-((1-methyl-2-phenoxyethyl)amino)-1-propanol) hydrochloride; 4-Hydroxy-α-[1-[(1-methyl-2-phenoxyethyl)amino]ethyl]benzenemethanol hydrochloride; p-Hydroxy-α-[1-[(1-methyl-2-phenoxyethyl)amino]ethyl]benzyl alcohol hydrochloride; (±)-Isoxsuprine hydrochloride
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Quality Control

Our Isoxsuprine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption.

Specification

Item Specification
Appearance White or almost white, crystalline powder
Identification (IR) Conforms to standard
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) 98.0% - 102.0% (on dried basis)
Loss on Drying ≤ 1.0%
Residue on Ignition ≤ 0.1%
Related Substances (HPLC) Total impurities ≤ 2.0% Any individual impurity ≤ 0.5%
Heavy Metals ≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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